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Carolina Luísa Cardoso Lemos
AuthID:
R-000-JQQ
Publications
Confirmed
To Validate
Document Source:
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Document Type:
All Document Types
Article (50)
Abstract (5)
Article in Press (4)
Review (2)
Unpublished (2)
Letter (1)
Correction (1)
Year Start - End:
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Order:
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Year Asc
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Cit. Scopus Dsc
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Results:
10
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50
Confirmed Publications: 65
61
TITLE:
Two novel functional mutations in the Na+,K+-ATPase alpha 2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes
Full Text
AUTHORS:
Castro, MJ; Nunes, B; de Vries, B;
Lemos, C
;
Vanmolkot, KRJ
;
van den Heuvel, JJMW
;
Temudo, T
; Barros, J;
Sequeiros, J
; Frants, RR; Koenderink, JB;
Pereira Monteiro, JM
;
van den Maagdenberg, AMJM
;
PUBLISHED:
2008
,
SOURCE:
CLINICAL GENETICS,
VOLUME:
73,
ISSUE:
1
INDEXED IN:
Scopus
WOS
CrossRef
:
17
IN MY:
ORCID
|
ResearcherID
62
TITLE:
Psychological follow-up of presymptomatic genetic testing for spinocerebellar ataxia type 2 (SCA2) in Cuba
Full Text
AUTHORS:
Paneque, M
;
Lemos, C
; Escalona, K; Prieto, L; Reynaldo, R; Velazquez, M; Quevedo, J; Santos, N; Almaguer, LE; Velazquez, L;
Sousa, A
;
Fleming, M
;
Sequeiros, J
;
PUBLISHED:
2007
,
SOURCE:
Journal of Genetic Counseling,
VOLUME:
16,
ISSUE:
4
INDEXED IN:
Scopus
CrossRef
:
11
IN MY:
ORCID
63
TITLE:
Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine
Full Text
AUTHORS:
Maria Jose Castro; Anine H Stam;
Carolina Lemos
;
Barros, José
;
Raquel G Gouveia
;
Isabel Pavao Martins
; Jan B Koenderink;
Kaate R J Vanmolkot
; Alexandre P Mendes; Rune R Frants; Michel D Ferrari;
Jorge Sequeiros
;
Jose M Pereira Monteiro
;
Arn M J M van den Maagdenberg
;
PUBLISHED:
2007
,
SOURCE:
JOURNAL OF HUMAN GENETICS,
VOLUME:
52,
ISSUE:
12
INDEXED IN:
Scopus
WOS
CrossRef
IN MY:
ORCID
|
ResearcherID
64
TITLE:
Migraine: Familial distribution in a Portuguese population [Enxaqueca: Distribuição familiar numa população portuguesa]
AUTHORS:
Lemos, C
; Castro, MJ; Mendonca, T;
Barros, José
;
Pereira Monteiro, JM
;
PUBLISHED:
2006
,
SOURCE:
Sinapse,
VOLUME:
6,
ISSUE:
1
INDEXED IN:
Scopus
IN MY:
ORCID
65
TITLE:
Novel recurrent mutation in ATP1A2 gene in a Portuguese family with familiar hemiplegic migraine type 2 [Nova mutação recorrente no gene ATP1A2 numa familia portuguesa com enxaqueca hemiplégica familiar tipo 2]
AUTHORS:
Castro, MJ; Barros, J;
Lemos, C
; Mendes, A; Vanmolkot, K; Frants, R;
Sequeiros, J
; Monteiro, JP; van den Maagdenberg, A;
PUBLISHED:
2006
,
SOURCE:
Sinapse,
VOLUME:
6,
ISSUE:
2
INDEXED IN:
Scopus
IN MY:
ORCID
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